Cleaning Validation

The **Cleaning Validation Engineer**is responsible for cleaning and process engineering and validation in the biotech and pharmaceutical industries. This individual will generate, execute, and report on testing for multiple phases of commissioning and qualification.

This position involves post cleaning validation monitoring, cleaning cycle development and cleaning validation in a cGMP facility. Experience in CIP/COP and manual cleaning validation activities is required. Experience troubleshooting CIP system failures, optimizing CIP/COP systems including manual processes and CIP equipment, developing CIP/COP Cycles is preferred. Experience Developing documents and SOPs and prepare reports is required. Must have experience analyze data, determine results and present conclusions and recommendations ensuring that projects are implemented in accordance with the agreed scope timelines, policies and procedures. Generate and resolve protocol discrepancies or deviations. Review GxP deliverables including specifications, drawings, procedural documents, master plans, and validation documentation. Train operations staff on protocols, procedures and technical details related to systems or processes. Organize, schedule and track validation projects in order to meet client requirements and agreed timelines.
- Hands-on experience with the following systems: CIP systems, cabinet washers, COP, manual cleaning is required.
- Experience with sampling techniques.
- Experience with development of manual cleaning protocols for Tablet press equipment is highly preferred.
- Working knowledge of cGMP requirements and strong written and verbal communication skills are required for this position.
- Experimental design and problem solving skills are preferred. Strong organizational skills and demonstrated ability to manage projects to completion are highly desired.
- Experience in discrepancy and non-conformance reporting, corrective action/preventive action systems and root cause analysis is preferred.

**Qualifications**:

- Strong Demonstrated problem solving and decision making skills
- Ability to understand and extract necessary information from technical documents
- Ability to handle complex projects
- Takes initiative to help drive projects forward and develop contingency plans when applicable
- Ability to work on cross-functional project teams
- Able to effectively manage workload and prioritize activities
- Excellent verbal and written communication skills
- Proven ability to review, interpret and make scientific conclusions and recommendations based on data
- Ability to work independently, handle multiple tasks simultaneously and to meet critical milestones and goals
- Effectively work within a team environment and interface with peers, management, etc.
- Strong computer skills, including experience using Microsoft Word, Excel, PowerPoint and Visio.

Since 1993, Hyde E+C has worked as an integral part of project teams for clients and equipment vendors in the pharmaceutical and biopharmaceutical industries, resulting in the successful construction, commissioning and validation of facilities and equipment. As a member of the Hyde team, you will be responsible for providing state-of-the-art custom solutions to leaders in our industry. As we continue to grow our operations globally, we strive to hire the best talent—men and women dedicated to quality and innovation. We offer a collaborative culture, challenging projects, and excellent compensation and benefits.

You will find the following values reflected in our company:

- Family
- Integrity
- Respect
- Wisdom
- Adventure

Hyde Engineering + Consulting is an equal opportunity, affirmative action employer.